|
NM_181486.4:c.756-2A>G
MANE Select
|
NP_852259.1:n.756-2A>G
|
|
ENST00000405440.7:c.756-2A>G
MANE Select
|
ENSP00000384152.3:n.756-2A>G
|
|
NM_000192.3:c.756-2A>G , LRG_670t1:c.756-2A>G
|
NP_000183.2:n.756-2A>G
|
|
NM_080717.2:c.606-2A>G
|
NP_542448.1:n.606-2A>G
|
|
NM_080717.3:c.606-2A>G
|
NP_542448.1:n.606-2A>G
|
|
NM_080717.4:c.606-2A>G
|
NP_542448.1:n.606-2A>G
|
|
NM_181486.2:c.756-2A>G
|
NP_852259.1:n.756-2A>G
|
|
ENST00000310346.8:c.756-2A>G
|
ENSP00000309913.4:n.756-2A>G
|
|
ENST00000349716.9:c.606-2A>G
|
ENSP00000337723.5:n.606-2A>G
|
|
ENST00000405440.6:c.756-2A>G
|
ENSP00000384152.2:n.756-2A>G
|
|
ENST00000526441.1:c.756-2A>G
|
ENSP00000433292.1:n.756-2A>G
|
|
XM_017019912.1:c.804-2A>G
|
XP_016875401.1:n.804-2A>G
|